Proudly supporting Cystic Fibrosis Australia


Supporting Cystic Fibrosis Australia
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Hi Everyone, We are raising much needed funds for Cystic Fibrosis Australia. Their work is really important, and we want to do what we can to help. But there is only so much we can do on our own. Our mascot is a very special person in our live's called "Flynn Morrison." Flynnie was born CF but in no way has he let him it hold him back in any aspect of his life. Flynnie lives his life to the fullest, practicing karate, playing soccer and learning guitar. Flynn, belongs to our good friend's Gav and Sammy Morrison and is big brother to his sister Chelsea. In aid of honouring our little mate, we are fundraising to find a cure for CF, and will be entering a team in the up and coming August, 2019 City to Surf. The "Pirtek Central Coast" team will consist of Big Gav, Sammy, along with my Husband Peter Bonvino and myself. Running, or in our case shuffling the 14km from start to finish. You can help too, by donating to our page. Any amount you can give makes a difference! You can also support me by encouraging others to get involved too. Please email the link to my page to your friends and family, or share it on social media. Thank you for your generosity and support -- it means the world to us. Together we can help Cystic Fibrosis Australia create the world we want to see. Much love and gratitude for your support. Big Gav, Sammy, Pete and Erin Flynn Morrison is our Hero.

Cystic Fibrosis Australia

Cystic Fibrosis (CF) primarily affects the lungs and digestive system because of a malfunction in the exocrine system, responsible for producing saliva, sweat, tears and mucus.

There is currently no cure. People with CF develop an abnormal amount of excessively thick and sticky mucus within the lungs, airways and the digestive system. The mucus causes impairment of the digestive functions of the pancreas and traps bacteria in the lungs resulting in recurrent infections which lead to irreversible damage. Lung failure is the major cause of death for someone with CF.

We advocate on behalf of our members to gain better access to services, obtain information or resources. On a larger scale we have been involved in several national campaigns to increase the rights of all people with cystic fibrosis.


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